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Publications by G A Bruns
Human Neutrophil Cytochrome B Light Chain (P22-Phox). Gene Structure, Chromosomal Location, and Mutations in Cytochrome-Negative Autosomal Recessive Chronic Granulomatous Disease.
Journal of Clinical Investigation
Medicine
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Chronic Granulomatous Disease With Neutrophil Membrane Cytochrome B Deficiency: Demonstration by Immunochemical Staining With Monoclonal Antibody.
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Successful Lung Transplant for Bronchiectasis in an Adult Male With Autosomal Recessive Chronic Granulomatous Disease With a Novel NF1 Gene Mutation
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Aspergillus Osteomyelitis in a Child Who Has P67-Phox-Deficient Chronic Granulomatous Disease.
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Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy
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Possible Application of Cytochrome B Gene for Human Identification = التطبيقات المحتملة لاستخدام الموقع الوراثي سيتوكروم ب ( Cytochrome B ) لتحديد الهوية البشرية
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Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
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Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts
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